Neural Tissue. PowerPoint Lecture Presentations prepared by Jason LaPres. Lone Star College North Harris Pearson Education, Inc.

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12 Neural Tissue PowerPoint Lecture Presentations prepared by Jason LaPres Lone Star College North Harris

An Introduction to the Nervous System Organs of the Nervous System Brain and spinal cord Sensory receptors of sense organs (eyes, ears, etc.) Nerves connect nervous system with other systems

12-1 Divisions of the Nervous System Anatomical Divisions of the Nervous System Central nervous system (CNS) Peripheral nervous system (PNS)

12-1 Divisions of the Nervous System The Central Nervous System (CNS) Functions of the CNS are to process and coordinate: Sensory data from inside and outside body Sends Motor commands to control activities of peripheral organs (e.g., skeletal muscles) Higher functions of brain intelligence, memory, learning, emotion

12-1 Divisions of the Nervous System The Peripheral Nervous System (PNS) Includes all neural tissue outside the CNS Functions of the PNS Deliver sensory information to the CNS Carry motor commands to peripheral tissues and systems peripheral nerves Consist of bundles of axons with connective tissues and blood vessels Carry sensory information and motor commands in PNS Cranial nerves connect to brain Spinal nerves attach to spinal cord

12-1 Divisions of the Nervous System Functional Divisions of the PNS Afferent division Carries sensory information From PNS sensory receptors to CNS Receptors Detect changes or respond to stimuli Neurons and specialized cells Complex sensory organs (e.g., eyes, ears)

12-1 Divisions of the Nervous System Functional Divisions of the PNS Efferent division Carries motor commands From CNS to PNS muscles and glands Effectors Respond to efferent signals Cells and organs

12-1 Divisions of the Nervous System The efferent division Somatic nervous system (SNS) Controls voluntary and involuntary (reflexes) muscle skeletal contractions Autonomic nervous system (ANS) Controls subconscious actions, contractions of smooth muscle and cardiac muscle, and glandular secretions Sympathetic division has a stimulating effect Parasympathetic division has a relaxing effect

12-2 Neurons Neurons The basic functional units of the nervous system The structure of neurons The multipolar neuron Common in the CNS Cell body (soma) Short, branched dendrites Long, single axon

12-2 Neurons The Cell Body Large nucleus and nucleolus Perikaryon (cytoplasm) Mitochondria (produce energy) RER and ribosomes (produce neurotransmitters)

12-2 Neurons The Cell Body Cytoskeleton Neurofilaments and neurotubules in place of microfilaments and microtubules Neurofibrils: bundles of neurofilaments that provide support for dendrites and axon Nissl bodies Dense areas of RER and ribosomes Make neural tissue appear gray (gray matter)

12-2 Neurons Dendrites Highly branched Dendritic spines Many fine processes Receive information from other neurons 80 90% of neuron surface area

12-2 Neurons The axon Is long Carries electrical signal (action potential) to the target end Axon structure is critical to function Axoplasm Cytoplasm of axon Contains neurofibrils, neurotubules, enzymes, organelles Axolemma Specialized cell membrane Covers the axoplasm

12-2 Neurons Structures of the Axon Axon hillock Thick section of cell body Attaches to initial segment Initial segment Attaches to axon hillock

12-2 Neurons Structures of the Axon Collaterals Branches of a single axon Telodendria Fine extensions of distal axon Synaptic terminals Tips of telodendria

Figure 12-1a The Anatomy of a Multipolar Neuron Dendrites Perikaryon Nucleus Cell body Axon Telodendria This color-coded figure shows the four general regions of a neuron.

Figure 12-1b The Anatomy of a Multipolar Neuron Dendritic branches Nissl bodies (RER and free ribosomes) Mitochondrion Axon hillock Initial segment of axon Golgi apparatus Neurofilament Nucleus Nucleolus Dendrite Axolemma Axon Telodendria Synaptic terminals See Figure 12 2 PRESYNAPTIC CELL An understanding of neuron function requires knowing its structural components. POSTSYNAPTIC CELL

12-2 Neurons The Structure of Neurons The synapse Area where a neuron communicates with another cell

12-2 Neurons The Structure of Neurons The synapse Presynaptic cell Neuron that sends message Postsynaptic cell Cell that receives message The synaptic cleft The small gap that separates the presynaptic membrane and the postsynaptic membrane

12-2 Neurons The Synapse The synaptic terminal Is expanded area of axon of presynaptic neuron Contains synaptic vesicles of neurotransmitters

12-2 Neurons Neurotransmitters Are chemical messengers Are released at presynaptic membrane Affect receptors of postsynaptic membrane Are broken down by enzymes Are reassembled at synaptic terminal

12-2 Neurons Types of Synapses Neuromuscular junction Synapse between neuron and muscle Neuroglandular junction Synapse between neuron and gland

Figure 12-2 The Structure of a Typical Synapse Telodendrion Synaptic terminal Mitochondrion Endoplasmic reticulum Synaptic vesicles Presynaptic membrane Postsynaptic membrane Synaptic cleft

12-2 Neurons Structural Classification of Neurons Anaxonic neurons Found in brain and sense organs Bipolar neurons Found in special sensory organs (sight, smell, hearing) Unipolar neurons Found in sensory neurons of PNS Multipolar neurons Common in the CNS Include all skeletal muscle motor neurons

12-2 Neurons Anaxonic Neurons Small All cell processes look alike Bipolar Neurons Are small One dendrite, one axon

12-2 Neurons Unipolar Neurons Also called pseudounipolar neurons Have very long axons Fused dendrites and axon Cell body to one side Multipolar Neurons Have very long axons Multiple dendrites, one axon

Figure 12-3a A Structural Classification of Neurons Anaxonic neuron Cell body Anaxonic neurons have more than two processes, but axons cannot be distinguished from dendrites.

Figure 12-3b A Structural Classification of Neurons Bipolar neuron Dendritic branches Dendrite Cell body Axon Synaptic terminals Bipolar neurons have two processes separated by the cell body.

Figure 12-3c A Structural Classification of Neurons Unipolar neuron Dendrites Initial segment Axon Cell body Axon Synaptic terminals Unipolar neurons have a single elongate process, with the cell body situated off to the side.

Figure 12-3d A Structural Classification of Neurons Multipolar neuron Dendrites Cell body Axon Synaptic terminals Multipolar neurons have more than two processes; there is a single axon and multiple dendrites.

12-2 Neurons Three Functional Classifications of Neurons 1. Sensory neurons Afferent neurons of PNS 2. Motor neurons Efferent neurons of PNS 3. Interneurons Association neurons

12-2 Neurons Functions of Sensory Neurons Monitor internal environment (visceral sensory neurons) Monitor effects of external environment (somatic sensory neurons) Structures of Sensory Neurons Unipolar Cell bodies grouped in sensory ganglia Processes (afferent fibers) extend from sensory receptors to CNS

12-2 Neurons Three Types of Sensory Receptors 1. Interoceptors Monitor internal systems (digestive, respiratory, cardiovascular, urinary, reproductive) Internal senses (taste, deep pressure, pain) 2. Exteroceptors External senses (touch, temperature, pressure) Distance senses (sight, smell, hearing) 3. Proprioceptors Monitor position and movement (skeletal muscles and joints)

12-2 Neurons Motor Neurons Carry instructions from CNS to peripheral effectors Via efferent fibers (axons) Two major efferent systems 1. Somatic nervous system (SNS) Includes all somatic motor neurons that innervate skeletal muscles 2. Autonomic (visceral) nervous system (ANS) Visceral motor neurons innervate all other peripheral effectors Smooth muscle, cardiac muscle, glands, adipose tissue

12-2 Neurons Motor Neurons Two groups of efferent axons Signals from CNS motor neurons to visceral effectors pass synapses at autonomic ganglia dividing axons into: Preganglionic fibers Postganglionic fibers

12-2 Neurons Interneurons Most are located in brain, spinal cord, and autonomic ganglia Between sensory and motor neurons Are responsible for: Distribution of sensory information Coordination of motor activity Are involved in higher functions Memory, planning, learning

12-3 Neuroglia Neuroglia Half the volume of the nervous system Many types of neuroglia in CNS and PNS Four Types of Neuroglia in the CNS 1. Ependymal cells Cells with highly branched processes; contact neuroglia directly 2. Astrocytes Large cell bodies with many processes 3. Oligodendrocytes Smaller cell bodies with fewer processes 4. Microglia Smallest and least numerous neuroglia with many finebranched processes

12-3 Neuroglia Ependymal Cells Form epithelium called ependyma Line central canal of spinal cord and ventricles of brain Secrete cerebrospinal fluid (CSF) Have cilia or microvilli that circulate CSF Monitor CSF Contain stem cells for repair

12-3 Neuroglia Astrocytes Maintain blood brain barrier (isolates CNS) Create three-dimensional framework for CNS Repair damaged neural tissue Guide neuron development Control interstitial environment

Figure 12-5b Neuroglia in the CNS CENTRAL CANAL Ependymal cells Gray matter Neurons Microglial cell A diagrammatic view of neural tissue in the CNS, showing relationships between neuroglia and neurons

Figure 12-5b Neuroglia in the CNS Myelinated axons Internode White matter Myelin (cut) Axon Oligodendrocyte Axolemma Astrocyte Node Unmyelinated axon Basement membrane Capillary A diagrammatic view of neural tissue in the CNS, showing relationships between neuroglia and neurons

12-3 Neuroglia Oligodendrocytes Form myelinated sheaths on axons Increases speed of action potentials Myelin insulates myelinated axons Makes nerves appear white Nodes and internodes Internodes - myelinated segments of axon Nodes (also called nodes of Ranvier) Gaps between internodes Where axons may branch

Figure 12-6a Schwann Cells and Peripheral Axons Axon hillock Axon Nucleus Myelinated internode Initial segment (unmyelinated) Dendrite Nodes Schwann cell nucleus Axon Neurilemma Axon Axolemma Myelin covering internode A myelinated axon, showing the organization of Schwann cells along the length of the axon. Also shown are stages in the formation of a myelin sheath by a single Schwann cell along a portion of a single axon.

12-3 Neuroglia Myelination White matter Regions of CNS with many myelinated nerves Gray matter Unmyelinated areas of CNS Microglia Migrate through neural tissue Clean up cellular debris, waste products, and pathogens

12-3 Neuroglia Neuroglia of the Peripheral Nervous System Ganglia Masses of neuron cell bodies Surrounded by neuroglia Found in the PNS

12-3 Neuroglia Neuroglia of the Peripheral Nervous System Satellite cells Also called amphicytes Surround ganglia Regulate environment around neuron

12-3 Neuroglia Neuroglia of the Peripheral Nervous System Schwann cells Also called neurilemma cells Form myelin sheath (neurilemma) around peripheral axons One Schwann cell sheaths one segment of axon Many Schwann cells sheath entire axon

Figure 12-6b Schwann Cells and Peripheral Axons Schwann cell Schwann cell nucleus Schwann cell #1 Schwann cell #2 Neurilemma Axons Schwann cell #3 nucleus Axons The enclosing of a group of unmyelinated axons by a single Schwann cell. A series of Schwann cells is required to cover the axons along their entire length.

12-3 Neuroglia Neurons and Neuroglia Neurons perform: All communication, information processing, and control functions of the nervous system Neuroglia preserve: Physical and biochemical structure of neural tissue Neuroglia are essential to: Survival and function of neurons

12-3 Neuroglia Neural Responses to Injuries Wallerian degeneration Axon distal to injury degenerates Schwann cells Form path for new growth Wrap new axon in myelin

12-3 Neuroglia Nerve Regeneration in CNS Limited by chemicals released by astrocytes that: Block growth Produce scar tissue

Figure 12-7 Peripheral Nerve Regeneration after Injury Fragmentation of axon and myelin occurs in distal stump. Axon Myelin Proximal stump Distal stump

Figure 12-7 Peripheral Nerve Regeneration after Injury Schwann cells form cord, grow into cut, and unite stumps. Macrophages engulf degenerating axon and myelin. Macrophage Cord of proliferating Schwann cells

Figure 12-7 Peripheral Nerve Regeneration after Injury Axon sends buds into network of Schwann cells and then starts growing along cord of Schwann cells.

Figure 12-7 Peripheral Nerve Regeneration after Injury Axon continues to grow into distal stump and is enclosed by Schwann cells.

12-4 Transmembrane Potential Ion Movements and Electrical Signals All plasma (cell) membranes produce electrical signals by ion movements Transmembrane potential is particularly important to neurons

12-4 Transmembrane Potential Five Main Membrane Processes in Neural Activities 1. Resting potential The transmembrane potential of resting cell 2. Graded potential Temporary, localized change in resting potential Caused by stimulus

12-4 Transmembrane Potential Five Main Membrane Processes in Neural Activities 3. Action potential Is an electrical impulse Produced by graded potential Propagates along surface of axon to synapse

12-4 Transmembrane Potential Five Main Membrane Processes in Neural Activities 4. Synaptic activity Releases neurotransmitters at presynaptic membrane Produces graded potentials in postsynaptic membrane 5. Information processing Response (integration of stimuli) of postsynaptic cell

Figure 12-8 An Overview of Neural Activities Resting potential stimulus produces Graded potential may produce Action potential Presynaptic neuron

Figure 12-8 An Overview of Neural Activities Action potential triggers Information processing Postsynaptic cell

12-4 Transmembrane Potential The Transmembrane Potential Three important concepts 1. The extracellular fluid (ECF) and intracellular fluid (cytosol) differ greatly in ionic composition Concentration gradient of ions (Na +, K + ) 2. Cells have selectively permeable membranes 3. Membrane permeability varies by ion A&P FLIX Resting Membrane Potential

12-4 Transmembrane Potential Passive Forces acting Across the Plasma Membrane Chemical gradients Concentration gradients (chemical gradient) of ions (Na +, K + ) Electrical gradients Separate charges of positive and negative ions Result in potential difference

Figure 12-9 The Resting Potential is the Transmembrane Potential of an Undisturbed Cell EXTRACELLULAR FLUID 70 30 0 +30 Cl mv K + leak channel 3 Na + Na + leak channel Plasma membrane Sodium potassium exchange pump CYTOSOL Protein 2 K + Protein Protein

12-4 Transmembrane Potential Electrical Currents and Resistance Electrical current Movement of charges to eliminate potential difference Resistance The amount of current a membrane restricts

12-4 Transmembrane Potential The Electrochemical Gradient For a particular ion (Na +, K + ) is: The sum of chemical and electrical forces Acting on the ion across a plasma membrane A form of potential energy

12-4 Transmembrane Potential Equilibrium Potential The transmembrane potential at which there is no net movement of a particular ion across the cell membrane Examples: K + = 90 mv Na + = +66 mv

Figure 12-10a Electrochemical Gradients for Potassium and Sodium Ions Potassium Ion Gradients At normal resting potential, an electrical gradient opposes the chemical gradient for potassium ions (K + ). The net electrochemical gradient tends to force potassium ions out of the cell. Potassium chemical gradient Potassium electrical gradient Net potassium electrochemical gradient Resting potential 70 mv Plasma membrane K + Cytosol Protein

Figure 12-10b Electrochemical Gradients for Potassium and Sodium Ions Potassium Ion Gradients If the plasma membrane were freely permeable to potassium ions, the outflow of K + would continue until the equilibrium potential ( 90 mv) was reached. Potassium chemical gradient Potassium electrical gradient Equilibrium potential 90 mv Plasma membrane K + Cytosol Protein

Figure 12-10c Electrochemical Gradients for Potassium and Sodium Ions Sodium Ion Gradients At the normal resting potential, chemical and electrical gradients combine to drive sodium ions (Na + ) into the cell. Sodium chemical gradient Sodium electrical gradient Net sodium electrochemical gradient Resting potential 70 mv Plasma membrane Cytosol Protein

Figure 12-10d Electrochemical Gradients for Potassium and Sodium Ions Sodium Ion Gradients If the plasma membrane were freely permeable to sodium ions, the influx of Na + would continue until the equilibrium potential (+66 mv) was reached. Sodium chemical gradient Sodium electrical gradient Equilibrium potential +66 mv Plasma membrane Cytosol Protein

12-4 Transmembrane Potential Active Forces across the Membrane Sodium potassium ATPase (exchange pump) Is powered by ATP Carries 3 Na + out and 2 K + in Balances passive forces of diffusion Maintains resting potential ( 70 mv)

12-4 Transmembrane Potential The Resting Potential Because the plasma membrane is highly permeable to potassium ions: The resting potential of approximately 70 mv is fairly close to 90 mv, the equilibrium potential for K + The electrochemical gradient for sodium ions is very large, but the membrane s permeability to these ions is very low Na + has only a small effect on the normal resting potential, making it just slightly less negative than the equilibrium potential for K +

12-4 Transmembrane Potential The Resting Potential The sodium potassium exchange pump ejects 3 Na + ions for every 2 K + ions that it brings into the cell It serves to stabilize the resting potential when the ratio of Na + entry to K + loss through passive channels is 3:2 At the normal resting potential, these passive and active mechanisms are in balance The resting potential varies widely with the type of cell A typical neuron has a resting potential of approximately 70 mv

12-4 Transmembrane Potential Changes in the Transmembrane Potential Transmembrane potential rises or falls In response to temporary changes in membrane permeability Resulting from opening or closing specific membrane channels

12-4 Transmembrane Potential Sodium and Potassium Channels Membrane permeability to Na + and K + determines transmembrane potential They are either passive or active

12-4 Transmembrane Potential Passive Channels (Leak Channels) Are always open Permeability changes with conditions Active Channels (Gated Channels) Open and close in response to stimuli At resting potential, most gated channels are closed

12-4 Transmembrane Potential Three States of Gated Channels 1. Closed, but capable of opening 2. Open (activated) 3. Closed, not capable of opening (inactivated)

12-4 Transmembrane Potential Three Classes of Gated Channels 1. Chemically gated channels 2. Voltage-gated channels 3. Mechanically gated channels

12-4 Transmembrane Potential Chemically Gated Channels Open in presence of specific chemicals (e.g., ACh) at a binding site Found on neuron cell body and dendrites

12-4 Transmembrane Potential Voltage-gated Channels Respond to changes in transmembrane potential Have activation gates (open) and inactivation gates (close) Characteristic of excitable membrane Found in neural axons, skeletal muscle sarcolemma, cardiac muscle

12-4 Transmembrane Potential Mechanically Gated Channels Respond to membrane distortion Found in sensory receptors (touch, pressure, vibration)

Figure 12-11a Gated Channels Chemically gated channel Resting state Presence of ACh ACh Binding site Channel closed Gated channel Channel open A chemically gated Na + channel that opens in response to the presence of ACh at a binding site.

Figure 12-11b Gated Channels Voltage-gated channel 70 mv Channel closed Inactivation gate 60 mv Channel open +30 mv Channel inactivated

Figure 12-11c Gated Channels Mechanically gated channel Channel closed Applied pressure Channel open Pressure removed Channel closed

12-4 Transmembrane Potential Transmembrane Potential Exists Across Plasma Membrane Because: Cytosol and extracellular fluid have different chemical/ionic balance The plasma membrane is selectively permeable Transmembrane Potential Changes with plasma membrane permeability In response to chemical or physical stimuli

12-4 Transmembrane Potential Graded Potentials Also called local potentials Changes in transmembrane potential That cannot spread far from site of stimulation Any stimulus that opens a gated channel Produces a graded potential

12-4 Transmembrane Potential Graded Potentials The resting state Opening sodium channel produces graded potential Resting membrane exposed to chemical Sodium channel opens Sodium ions enter the cell Transmembrane potential rises Depolarization occurs

Figure 12-12 Graded Potentials Initial segment Resting State Resting membrane with closed chemically gated sodium ion channels 70 mv EXTRA- CELLULAR FLUID CYTOSOL

12-4 Transmembrane Potential Graded Potentials Depolarization A shift in transmembrane potential toward 0 mv Movement of Na + through channel Produces local current Depolarizes nearby plasma membrane (graded potential) Change in potential is proportional to stimulus

Figure 12-12 Graded Potentials Stimulus applied here Stimulation Membrane exposed to chemical that opens the sodium ion channels 65 mv

Figure 12-12 Graded Potentials Graded Potential Spread of sodium ions inside plasma membrane produces a local current that depolarizes adjacent portions of the plasma membrane Local current 60 mv 65 mv 70 mv Local current

12-4 Transmembrane Potential Graded Potentials Whether depolarizing or hyperpolarizing, share four basic characteristics 1. The transmembrane potential is most changed at the site of stimulation, and the effect decreases with distance 2. The effect spreads passively, due to local currents

12-4 Transmembrane Potential Graded Potentials Whether depolarizing or hyperpolarizing, share four basic characteristics 3. The graded change in transmembrane potential may involve either depolarization or hyperpolarization The properties and distribution of the membrane channels involved determine the nature of the change For example, in a resting membrane, the opening of sodium channels causes depolarization, whereas the opening of potassium channels causes hyperpolarization The change in transmembrane potential reflects whether positive charges enter or leave the cell 4. The stronger the stimulus, the greater the change in the transmembrane potential and the larger the area affected

12-4 Transmembrane Potential Graded Potentials Repolarization When the stimulus is removed, transmembrane potential returns to normal Hyperpolarization Increasing the negativity of the resting potential Result of opening a potassium channel Opposite effect of opening a sodium channel Positive ions move out, not into cell

Figure 12-13 Depolarization, Repolarization, and Hyperpolarization Chemical stimulus applied Chemical stimulus removed Repolarization Chemical stimulus applied Chemical stimulus removed Transmembrane potential (mv) Resting potential Depolarization Hyperpolarization Return to resting potential

12-4 Transmembrane Potential Graded Potentials Effects of graded potentials At cell dendrites or cell bodies Trigger specific cell functions For example, exocytosis of glandular secretions At motor end plate Release ACh into synaptic cleft

12-5 Action Potential Action Potentials Propagated changes in transmembrane potential Affect an entire excitable membrane Link graded potentials at cell body with motor end plate actions

12-5 Action Potential Initiating Action Potential Initial stimulus A graded depolarization of axon hillock large enough (10 to 15 mv) to change resting potential ( 70 mv) to threshold level of voltage-gated sodium channels ( 60 to 55 mv)

12-5 Action Potential Initiating Action Potential All-or-none principle If a stimulus exceeds threshold amount The action potential is the same No matter how large the stimulus Action potential is either triggered, or not

Figure 12-14 Generation of an Action Potential Resting Potential 70 mv The axolemma contains both voltagegated sodium channels and voltagegated potassium channels that are closed when the membrane is at the resting potential. KEY = Sodium ion = Potassium ion

12-5 Action Potential Four Steps in the Generation of Action Potentials Step 1: Depolarization to threshold Step 2: Activation of Na + channels Step 3: Inactivation of Na + channels and activation of K + channels Step 4: Return to normal permeability

12-5 Action Potential Step 1: Depolarization to threshold Step 2: Activation of Na + channels Rapid depolarization Na + ions rush into cytoplasm Inner membrane changes from negative to positive

Figure 12-14 Generation of an Action Potential Depolarization to Threshold 60 mv Local current KEY = Sodium ion = Potassium ion

Figure 12-14 Generation of an Action Potential Activation of Sodium Channels and Rapid Depolarization +10 mv KEY = Sodium ion = Potassium ion

12-5 Action Potential Step 3: Inactivation of Na + channels and activation of K + channels At +30 mv Inactivation gates close (Na + channel inactivation) K + channels open Repolarization begins

Figure 12-14 Generation of an Action Potential Inactivation of Sodium Channels and Activation of Potassium Channels +30 mv KEY = Sodium ion = Potassium ion

12-5 Action Potential Step 4: Return to normal permeability K + channels begin to close When membrane reaches normal resting potential ( 70 mv) K + channels finish closing Membrane is hyperpolarized to 90 mv Transmembrane potential returns to resting level Action potential is over

Figure 12-14 Generation of an Action Potential Closing of Potassium Channels 90 mv KEY = Sodium ion = Potassium ion

12-5 Action Potential The Refractory Period The time period From beginning of action potential To return to resting state During which membrane will not respond normally to additional stimuli A&P FLIX Generation of an Action Potential

12-5 Action Potential Absolute Refractory Period Sodium channels open or inactivated No action potential possible Relative Refractory Period Membrane potential almost normal Very large stimulus can initiate action potential

12-5 Action Potential Powering the Sodium Potassium Exchange Pump To maintain concentration gradients of Na + and K + over time Requires energy (1 ATP for each 2 K + /3 Na + exchange) Without ATP Neurons stop functioning

Figure 12-14 Generation of an Action Potential Sodium channels close, voltagegated potassium channels open D E P O L A R I Z A T I O N R E P O L A R I Z A T I O N Transmembrane potential (mv) Resting potential Threshold Graded potential causes threshold Voltage-gated sodium ion channels open All channels closed ABSOLUTE REFRACTORY PERIOD RELATIVE REFRACTORY PERIOD Cannot respond Responds only to a larger than normal stimulus Time (msec)

12-5 Action Potential Propagation of Action Potentials Propagation Moves action potentials generated in axon hillock Along entire length of axon Two methods of propagating action potentials 1. Continuous propagation (unmyelinated axons) 2. Saltatory propagation (myelinated axons)

12-5 Action Potential Continuous Propagation Of action potentials along an unmyelinated axon Affects one segment of axon at a time Steps in propagation Step 1: Action potential in segment 1 Depolarizes membrane to +30 mv Local current Step 2: Depolarizes second segment to threshold Second segment develops action potential

Figure 12-15 Continuous Propagation of an Action Potential along an Unmyelinated Axon As an action potential develops at the initial segment 1, the transmembrane potential at this site depolarizes to +30 mv. Action potential Na + +30 mv 70 mv Extracellular Fluid 70 mv Cell membrane Cytosol

Figure 12-15 Continuous Propagation of an Action Potential along an Unmyelinated Axon As the sodium ions entering at 1 spread away from the open voltage-gated channels, a graded depolarization quickly brings the membrane in segment 2 to threshold. Graded depolarization 60 mv 70 mv Local current

12-5 Action Potential Continuous Propagation Steps in propagation Step 3: First segment enters refractory period Step 4: Local current depolarizes next segment Cycle repeats Action potential travels in one direction (1 m/sec)

Figure 12-15 Continuous Propagation of an Action Potential along an Unmyelinated Axon An action potential now occurs in segment 2 while segment 1 beings repolarization. Repolarization (refractory) Na + +30 mv 70 mv

Figure 12-15 Continuous Propagation of an Action Potential along an Unmyelinated Axon As the sodium ions entering at segment 2 spread laterally, a graded depolarization quickly brings the membrane in segment 3 to threshold, and the cycle is repeated. 60 mv Local current

12-5 Action Potential Saltatory Propagation Action potential along myelinated axon Faster and uses less energy than continuous propagation Myelin insulates axon, prevents continuous propagation Local current jumps from node to node Depolarization occurs only at nodes

Figure 12-16 Saltatory Propagation along a Myelinated Axon An action potential has occurred at the initial segment 1. +30 mv 70 mv 70 mv Extracellular Fluid Na + Myelinated internode Myelinated internode Myelinated internode Plasma membrane Cytosol

Figure 12-16 Saltatory Propagation along a Myelinated Axon A local current produces a graded depolarization that brings the axolemma at the next node to threshold. 60 mv 70 mv Local current

Figure 12-16 Saltatory Propagation along a Myelinated Axon An action potential develops at node 2. Repolarization (refractory) +30 mv 70 mv Na +

Figure 12-16 Saltatory Propagation along a Myelinated Axon A local current produces a graded depolarization that brings the axolemma at node 3 to threshold. 60 mv Local current A&P FLIX Propagation of an Action Potential

12-6 Axon Diameter and Speed Axon Diameter and Propagation Speed Ion movement is related to cytoplasm concentration Axon diameter affects action potential speed The larger the diameter, the lower the resistance

12-6 Axon Diameter and Speed Three Groups of Axons 1. Type A fibers 2. Type B fibers 3. Type C fibers These groups are classified by: Diameter Myelination Speed of action potentials

12-6 Axon Diameter and Speed Type A Fibers Myelinated Large diameter High speed (140 m/sec) Carry rapid information to/from CNS For example, position, balance, touch, and motor impulses

12-6 Axon Diameter and Speed Type B Fibers Myelinated Medium diameter Medium speed (18 m/sec) Carry intermediate signals For example, sensory information, peripheral effectors

12-6 Axon Diameter and Speed Type C Fibers Unmyelinated Small diameter Slow speed (1 m/sec) Carry slower information For example, involuntary muscle, gland controls

12-6 Axon Diameter and Speed Information Information travels within the nervous system As propagated electrical signals (action potentials) The most important information (vision, balance, motor commands) Is carried by large-diameter, myelinated axons

12-7 Synapses Synaptic Activity Action potentials (nerve impulses) Are transmitted from presynaptic neuron To postsynaptic neuron (or other postsynaptic cell) Across a synapse

12-7 Synapses Two Types of Synapses 1. Electrical synapses Direct physical contact between cells 2. Chemical synapses Signal transmitted across a gap by chemical neurotransmitters

12-7 Synapses Electrical Synapses Are locked together at gap junctions (connexons) Allow ions to pass between cells Produce continuous local current and action potential propagation Are found in areas of brain, eye, ciliary ganglia

12-7 Synapses Chemical Synapses Are found in most synapses between neurons and all synapses between neurons and other cells Cells not in direct contact Action potential may or may not be propagated to postsynaptic cell, depending on: Amount of neurotransmitter released Sensitivity of postsynaptic cell

12-7 Synapses Two Classes of Neurotransmitters 1. Excitatory neurotransmitters Cause depolarization of postsynaptic membranes Promote action potentials 2. Inhibitory neurotransmitters Cause hyperpolarization of postsynaptic membranes Suppress action potentials

12-7 Synapses The Effect of a Neurotransmitter On a postsynaptic membrane Depends on the receptor Not on the neurotransmitter For example, acetylcholine (ACh) Usually promotes action potentials But inhibits cardiac neuromuscular junctions

12-7 Synapses Cholinergic Synapses Any synapse that releases ACh at: 1. All neuromuscular junctions with skeletal muscle fibers 2. Many synapses in CNS 3. All neuron-to-neuron synapses in PNS 4. All neuromuscular and neuroglandular junctions of ANS parasympathetic division

12-7 Synapses Events at a Cholinergic Synapse 1. Action potential arrives, depolarizes synaptic terminal 2. Calcium ions enter synaptic terminal, trigger exocytosis of ACh 3. ACh binds to receptors, depolarizes postsynaptic membrane 4. ACh removed by AChE AChE breaks ACh into acetate and choline

Figure 12-17 Events in the Functioning of a Cholinergic Synapse An action potential arrives and depolarizes the synaptic terminal Presynaptic neuron Synaptic vesicles ER Action potential EXTRACELLULAR FLUID Synaptic terminal AChE Initial segment POSTSYNAPTIC NEURON

Figure 12-17 Events in the Functioning of a Cholinergic Synapse Extracellular Ca 2+ enters the synaptic terminal, triggering the exocytosis of ACh ACh Ca2+ Ca 2+ Synaptic cleft Chemically gated sodium ion channels

Figure 12-17 Events in the Functioning of a Cholinergic Synapse ACh binds to receptors and depolarizes the postsynaptic membrane Initiation of action potential if threshold is reached at the initial segment Na + Na + Na + Na + Na +

Figure 12-17 Events in the Functioning of a Cholinergic Synapse ACh is removed by AChE Propagation of action potential (if generated)

12-7 Synapses Synaptic Delay A synaptic delay of 0.2 0.5 msec occurs between: Arrival of action potential at synaptic terminal And effect on postsynaptic membrane Fewer synapses mean faster response Reflexes may involve only one synapse

12-7 Synapses Synaptic Fatigue Occurs when neurotransmitter cannot recycle fast enough to meet demands of intense stimuli Synapse inactive until ACh is replenished

Table 12-4 Synaptic Activity Mitochondrion Acetylcholine Synaptic vesicle SYNAPTIC TERMINAL Choline Acetate Acetylcholinesterase (AChE) SYNAPTIC CLEFT POSTSYNAPTIC MEMBRANE ACh receptor

12-8 Neurotransmitters and Neuromodulators Other Neurotransmitters At least 50 neurotransmitters other than ACh, including: Biogenic amines Amino acids Neuropeptides Dissolved gases

12-8 Neurotransmitters and Neuromodulators Important Neurotransmitters Other than acetylcholine Norepinephrine (NE) Dopamine Serotonin Gamma aminobutyric acid (GABA)

12-8 Neurotransmitters and Neuromodulators Norepinephrine (NE) Released by adrenergic synapses Excitatory and depolarizing effect Widely distributed in brain and portions of ANS Dopamine A CNS neurotransmitter May be excitatory or inhibitory Involved in Parkinson s disease and cocaine use

12-8 Neurotransmitters and Neuromodulators Serotonin A CNS neurotransmitter Affects attention and emotional states Gamma Aminobutyric Acid (GABA) Inhibitory effect Functions in CNS Not well understood

12-8 Neurotransmitters and Neuromodulators Chemical Synapse The synaptic terminal releases a neurotransmitter that binds to the postsynaptic plasma membrane Produces temporary, localized change in permeability or function of postsynaptic cell Changes affect cell, depending on nature and number of stimulated receptors

12-8 Neurotransmitters and Neuromodulators Many Drugs Affect nervous system by stimulating receptors that respond to neurotransmitters Can have complex effects on perception, motor control, and emotional states

12-8 Neurotransmitters and Neuromodulators Neuromodulators Other chemicals released by synaptic terminals Similar in function to neurotransmitters Characteristics of neuromodulators Effects are long term, slow to appear Responses involve multiple steps, intermediary compounds Affect presynaptic membrane, postsynaptic membrane, or both Released alone or with a neurotransmitter

12-8 Neurotransmitters and Neuromodulators Neuropeptides Neuromodulators that bind to receptors and activate enzymes Opioids Neuromodulators in the CNS Bind to the same receptors as opium or morphine Relieve pain

12-8 Neurotransmitters and Neuromodulators Four Classes of Opioids 1. Endorphins 2. Enkephalins 3. Endomorphins 4. Dynorphins

12-8 Neurotransmitters and Neuromodulators How Neurotransmitters and Neuromodulators Work Direct effects on membrane channels For example, ACh, glycine, aspartate Indirect effects via G proteins For example, E, NE, dopamine, histamine, GABA Indirect effects via intracellular enzymes For example, lipid-soluble gases (NO, CO)

12-8 Neurotransmitters and Neuromodulators Direct Effects Ionotropic effects Open/close gated ion channels

Figure 12-18a Mechanisms of Neurotransmitter Function Direct effects Examples: ACh, glutamate, aspartate ACh Binding site Gated channel

12-8 Neurotransmitters and Neuromodulators Indirect Effects G Proteins Work through second messengers Enzyme complex that binds GTP Link between neurotransmitter (first messenger) and second messenger Activate enzyme adenylate cyclase Which produces second messenger cyclic-amp (camp)

Figure 12-18b Mechanisms of Neurotransmitter Function Indirect effects via G proteins Examples: E, NE, dopamine, histamine, GABA Neurotransmitter Receptor G protein (inactive) G protein (active) Adenylate cyclase Opens ion channels Activates enzymes that change cell metabolism and activity

12-8 Neurotransmitters and Neuromodulators Indirect Effects Intracellular Receptors Lipid-soluble gases (NO, CO) Bind to enzymes in brain cells

Figure 12-18c Mechanisms of Neurotransmitter Function Indirect effects via intracellular enzymes Examples: Nitric oxide, carbon monoxide Nitric oxide Opens ion channels Production of secondary messengers Activation of enzymes Changes in cell metabolism and activity

12-9 Information Processing Information Processing At the simplest level (individual neurons) Many dendrites receive neurotransmitter messages simultaneously Some excitatory, some inhibitory Net effect on axon hillock determines if action potential is produced

12-9 Information Processing Postsynaptic Potentials Graded potentials developed in a postsynaptic cell In response to neurotransmitters Two Types of Postsynaptic Potentials 1. Excitatory postsynaptic potential (EPSP) Graded depolarization of postsynaptic membrane 2. Inhibitory postsynaptic potential (IPSP) Graded hyperpolarization of postsynaptic membrane

12-9 Information Processing Inhibition A neuron that receives many IPSPs Is inhibited from producing an action potential Because the stimulation needed to reach threshold is increased Summation To trigger an action potential One EPSP is not enough EPSPs (and IPSPs) combine through summation 1. Temporal summation 2. Spatial summation

12-9 Information Processing Temporal Summation Multiple times Rapid, repeated stimuli at one synapse Spatial Summation Multiple locations Many stimuli, arrive at multiple synapses

Figure 12-19a Temporal and Spatial Summation First stimulus arrives Second stimulus arrives and is added to the first stimulus Action potential is generated FIRST STIMULUS SECOND STIMULUS ACTION POTENTIAL PROPAGATION Initial segment Threshold reached Temporal Summation. Temporal summation occurs on a membrane that receives two depolarizing stimuli from the same source in rapid succession. The effects of the second stimulus are added to those of the first.

Figure 12-19b Temporal and Spatial Summation Two stimuli arrive simultaneously Action potential is generated TWO SIMULTANEOUS STIMULI ACTION POTENTIAL PROPAGATION Threshold reached Spatial Summation. Spatial summation occurs when sources of stimulation arrive simultaneously, but at different locations. Local currents spread the depolarizing effects, and areas of overlap experience the combined effects.

12-9 Information Processing Facilitation A neuron becomes facilitated As EPSPs accumulate Raising transmembrane potential closer to threshold Until a small stimulus can trigger action potential

12-9 Information Processing Summation of EPSPs and IPSPs Neuromodulators and hormones Can change membrane sensitivity to neurotransmitters Shifting balance between EPSPs and IPSPs

Figure 12-20 Interactions between EPSPs and IPSPs Time 2: Hyperpolarizing stimulus applied Stimulus removed Time 3: Hyperpolarizing stimulus applied EPSP Resting potential IPSP Resting potential EPSP IPSP Time 1: Depolarizing stimulus applied Stimulus removed Time 3: Depolarizing stimulus applied Stimuli removed

12-9 Information Processing Axoaxonic Synapses Synapses between the axons of two neurons Presynaptic inhibition Action of an axoaxonic synapse at a synaptic terminal that decreases the neurotransmitter released by presynaptic membrane Presynaptic facilitation Action of an axoaxonic synapse at a synaptic terminal that increases the neurotransmitter released by presynaptic membrane

Figure 12-21a Presynaptic Inhibition and Presynaptic Facilitation Action potential arrives GABA release Inactivation of calcium channels 1. Action potential arrives Ca 2+ 2. Less calcium enters 3. Less neurotransmitter released 4. Reduced effect on postsynaptic membrane Presynaptic inhibition

Figure 12-21b Presynaptic Inhibition and Presynaptic Facilitation Action potential arrives Serotonin release Activation of calcium channels 1. Action potential arrives Ca 2+ Ca 2+ 2. More calcium enters 3. More neurotransmitter released 4. Increased effect on postsynaptic membrane Presynaptic facilitation

12-9 Information Processing Frequency of Action Potentials Information received by a postsynaptic cell may be simply the frequency of action potentials received Rate of Generation of Action Potentials Frequency of action potentials depends on degree of depolarization above threshold Holding membrane above threshold level Has same effect as a second, larger stimulus Reduces relative refractory period

12-9 Information Processing In the Nervous System A change in transmembrane potential that determines whether or not action potentials are generated is the simplest form of information processing

12-9 Information Processing Summary Information is relayed in the form of action potentials In general, the degree of sensory stimulation or the strength of the motor response is proportional to the frequency of action potentials The neurotransmitters released at a synapse may have either excitatory or inhibitory effects The effect on the axon s initial segment reflects a summation of the stimuli that arrive at any moment The frequency of generation of action potentials is an indication of the degree of sustained depolarization at the axon hillock

12-9 Information Processing Summary Neuromodulators Can alter either the rate of neurotransmitter release or the response of a postsynaptic neuron to specific neurotransmitters Neurons May be facilitated or inhibited by extracellular chemicals other than neurotransmitters or neuromodulators

12-9 Information Processing Summary The response of a postsynaptic neuron to the activation of a presynaptic neuron can be altered by: 1. The presence of neuromodulators or other chemicals that cause facilitation or inhibition at the synapse 2. Activity under way at other synapses affecting the postsynaptic cell 3. Modification of the rate of neurotransmitter release through presynaptic facilitation or presynaptic inhibition